Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TATTGCTGTTAAGACTCTCTCATTA[A/G]TTGGACAATTGCAGACTGAAACGCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
|||||||||||||||||||||
Literature Links: |
MCMDC2 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
MCMDC2 - minichromosome maintenance domain containing 2 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001136160.1 | 389 | Missense Mutation | ATT,GTT | I,V 87 | NP_001129632.1 | |
NM_001136161.1 | 389 | Missense Mutation | ATT,GTT | I,V 87 | NP_001129633.1 | |
NM_173518.4 | 389 | Missense Mutation | ATT,GTT | I,V 87 | NP_775789.3 | |
XM_005251174.2 | 389 | Missense Mutation | ATT,GTT | I,V 24 | XP_005251231.1 | |
XM_006716427.3 | 389 | Missense Mutation | ATT,GTT | I,V 69 | XP_006716490.1 | |
XM_006716429.2 | 389 | Missense Mutation | ATT,GTT | I,V 87 | XP_006716492.1 | |
XM_006716433.3 | 389 | UTR 5 | XP_006716496.1 | |||
XM_011517467.2 | 389 | Missense Mutation | ATT,GTT | I,V 87 | XP_011515769.1 | |
XM_011517468.2 | 389 | Missense Mutation | ATT,GTT | I,V 87 | XP_011515770.1 | |
XM_011517469.2 | 389 | Missense Mutation | ATT,GTT | I,V 87 | XP_011515771.1 | |
XM_017013140.1 | 389 | UTR 5 | XP_016868629.1 |